EVA NEXUS™ Posterior 23G TDC Pack 9311.23G01

GUDID 18717872035106

D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.

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• Primary Device ID: 18717872035106
• NIH Device Record Key: 5c58372f-6008-443b-b1e7-806f2c9803ba
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EVA NEXUS™ Posterior 23G TDC Pack
• Version Model Number: 9311.23G01
• Catalog Number: 9311.23G01
• Company DUNS: 407522184
• Company Name: D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
• Device Count: 6
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08717872035109 [Primary]
GS1	18717872035106 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K213467

FDA Product Code

• HQE: Instrument, Vitreous Aspiration And Cutting, Ac-Powered

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-02-29
• Device Publish Date: 2024-02-21

On-Brand Devices [EVA NEXUS™ Posterior 23G TDC Pack]

• 18717872032846: 9310.23G01
• 18717872034734: 9310.23G01-00
• 18717872035304: 9311.23G01-00
• 18717872035106: 9311.23G01